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Structure of 245115-25-7
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This chiral cyclopentane-based amino acid derivative features a protected amine and carboxylic acid group, enabling direct incorporation into peptide synthesis workflows. The (1R,2R) stereochemistry ensures high diastereoselectivity in cyclization reactions, while the tert-butoxycarbonyl (Boc) group provides stability under standard conditions and facilitates selective deprotection.
(1R,2R)-2-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid serves as a stereochemically defined building block for cyclopentane-based peptidomimetics and bioactive scaffolds. The Boc-protected amine enables straightforward deprotection and coupling in solid-phase and solution-phase synthesis. Its rigid cyclopentane core provides conformational constraint, enhancing target selectivity in medicinal chemistry applications. The carboxylic acid functionality facilitates direct amidation or esterification, supporting versatile downstream derivatization. Bench-stable and easily purified by standard chromatographic methods, it functions reliably in multi-step synthetic sequences.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: